Pseudomonas aeruginosa virulence target
Lead Optimization
Microbiotix’s unique approach to targeting drug-resistant Gram-negative
bacteria focuses on bacterial virulence, specifically the type III secretion
system of Pseudomonas aeruginosa. The novel inhibitors, discovered by
Microbiotix scientists, have been shown to reverse the pathogen’s disruption
of the host innate immune response to infection and are not subject to
efflux or existing antibiotic resistance mechanisms.
During infection, this system secretes toxins that cause destruction
primarily of neutrophils and macrophages, disrupting the host’s immune
response, thus promoting the establishment and dissemination of infections.
Mechanism: Inhibition of type III secretion system (T3SS)
Needle type projection (PscF) delivers toxins into host cells,
destroying macrophages and neutrophils, thus disrupting the host’s immune response
T3SS inhibitors, targeting PscF, reverse this process, preventing
the establishment and dissemination of infection, while avoiding
efflux and existing resistance mechanisms
Prevention and treatment of ventilator-associated pneumonia (VAP) caused by P. aeruginosa
VAP is an urgent medical need.
Common infection in critically ill patients.
High mortality rates: >35% for MDR strains.
Elevated healthcare costs: ~ $40,000 per episode.
Novel anti-virulence approach.
Strong partnerships
Microbiotix was among the first recipients of funding ($3.2 million) from CARB-X (Combating Antibiotic Resistant Bacteria Biopharmaceutical Accelerator).
Microbiotix and its development partner, the UK’s AMR Centre, have
combined resources and antimicrobial R&D expertise to accelerate the
development of Microbiotix’s lead bacterial anti-virulence candidate.